Canonical Allele Identifier: CA2059113325
Gene: NUP37 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102119753G>A , CM000674.2:g.102119753G>A GRCh38
NC_000012.11:g.102513531G>A , CM000674.1:g.102513531G>A GRCh37
NC_000012.10:g.101037661G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000552283.6:c.-66+297C>T MANE Select ENSP00000448054.1:n.-66+297C>T
ENST00000543021.5:n.40+297C>T
ENST00000548994.1:n.41+297C>T
ENST00000551200.5:n.42+297C>T
ENST00000551744.2:c.-66+297C>T ENSP00000448086.1:n.-66+297C>T
ENST00000552283.5:c.-66+297C>T ENSP00000448054.1:n.-66+297C>T
XM_005269144.2:c.-66+297C>T XP_005269201.1:n.-66+297C>T
XR_944712.1:n.90+297C>T
NM_024057.3:c.-66+297C>T NP_076962.2:n.-66+297C>T
XR_944712.2:n.82+297C>T
NM_024057.4:c.-66+297C>T MANE Select NP_076962.2:n.-66+297C>T